Figure - PMC

Skip to main content

An official website of the United States government

Here's how you know

Here's how you know

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

View full-text article in PMC

. 2018 Feb 16;8:3176. doi: 10.1038/s41598-018-21621-5

Search in PMC
Search in PubMed
View in NLM Catalog
Add to search

© The Author(s) 2018

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

PMC Copyright notice

Immunofluorescent staining for CD86 and Arg-1. Lesion epicenter immunofluorescent staining: (A) On 1 day after SCI, the expressions of CD86 was significantly suppressed by TUDCA. However, the expressions of Arg-1 were not significantly different. (B) On 3 day after SCI, the expressions of CD86 were significantly suppressed by TUDCA and the expressions of Arg-1 were significantly induced by TUDCA. (C) On 7 days after SCI, the expressions of CD86 were significantly suppressed by TUDCA and the expressions of Arg-1 were significantly induced by TUDCA. (Scale bar = 80 µm). (D) Quantitative analysis of the fluorescence intensity for CD86. (E) Analysis of the quantitative fluorescence intensity for Arg-1. Results are the mean ± SD of triplicate experiments: **p < 0.01, and ***p < 0.001 significant difference as compared to the control group for each time by one-way ANOVA followed by Tukey’s post hoc analysis.